WO2020151538A1 - Instrument de chargement d'implant, dispositif de compression et système de chargement - Google Patents

Instrument de chargement d'implant, dispositif de compression et système de chargement Download PDF

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Publication number
WO2020151538A1
WO2020151538A1 PCT/CN2020/072134 CN2020072134W WO2020151538A1 WO 2020151538 A1 WO2020151538 A1 WO 2020151538A1 CN 2020072134 W CN2020072134 W CN 2020072134W WO 2020151538 A1 WO2020151538 A1 WO 2020151538A1
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WO
WIPO (PCT)
Prior art keywords
implant
protective tube
connecting portion
protective
guide cover
Prior art date
Application number
PCT/CN2020/072134
Other languages
English (en)
Chinese (zh)
Inventor
梅杰
刘美辰
吴旭闻
桂宝珠
陈国明
李�雨
Original Assignee
上海微创心通医疗科技有限公司
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 上海微创心通医疗科技有限公司 filed Critical 上海微创心通医疗科技有限公司
Priority to EP20745653.4A priority Critical patent/EP3915520B1/fr
Priority to KR1020217026401A priority patent/KR102640498B1/ko
Publication of WO2020151538A1 publication Critical patent/WO2020151538A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/95—Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/9522—Means for mounting a stent or stent-graft onto or into a placement instrument
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/95—Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/9522—Means for mounting a stent or stent-graft onto or into a placement instrument
    • A61F2/9525—Means for mounting a stent or stent-graft onto or into a placement instrument using a funnel
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
    • A61F2/2412—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body with soft flexible valve members, e.g. tissue valves shaped like natural valves
    • A61F2/2418—Scaffolds therefor, e.g. support stents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
    • A61F2/2442—Annuloplasty rings or inserts for correcting the valve shape; Implants for improving the function of a native heart valve
    • A61F2/2466—Delivery devices therefor
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
    • A61F2/2427—Devices for manipulating or deploying heart valves during implantation
    • A61F2/2436—Deployment by retracting a sheath
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/844—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents folded prior to deployment

Definitions

  • the invention relates to the field of medical equipment, and in particular to a loading tool, a compression device and a loading system for implants.
  • Interventional aortic valve placement is a brand-new minimally invasive valve replacement technology developed internationally in recent years. Its principle is that the valve prosthesis (which includes a stent) is loaded into the delivery device and delivered to it through a catheter. At the aortic root, after the stent is released, it can ensure that the valve prosthesis is fixed to the aortic valve annulus, replacing the degraded original valve, and improving the patient's heart function.
  • This technology can treat aortic valvular disease without opening the chest and the heart is beating, avoiding the huge trauma caused by previous surgical thoracotomy and cardiac arrest.
  • This technique requires compressing the stent to a small diameter to load into the delivery catheter.
  • the stent or the valve on the stent is prone to stent damage or valve damage due to excessive compression, uneven compression, or local accidental bending, which will eventually lead to defects in the function of the stent or valve or reduced service life, and may even fail to implant and work normally .
  • the self-expanding stent is loaded, the self-expanding stent is less likely to be fixed and compressed due to its own tension, and it is more likely to be damaged or broken, making it more difficult to load.
  • the technical requirements for the loading personnel are higher.
  • it also invisibly prolongs the implantation operation time and increases the operation risk.
  • the purpose of the present invention is to provide a loading tool, a compression device and a loading system for an implant, so as to solve the problem that the existing loading device requires multiple operations during use.
  • the present invention provides an implant loading tool, which is used to cooperate with an implant compression device to load an implant into a delivery device, the implant loading tool includes :
  • a protective tube for the delivery device to pass through the protective tube has a relatively proximal end and a distal end, the proximal end is used for the implant to penetrate;
  • the protective tube is configured to be connected to the compression device of the implant through the first connecting portion, while remaining coaxial with the compression device of the implant.
  • the delivery device includes a sheath tube, and the protective tube is provided with an anti-drop structure, and the anti-drop structure is used to limit the sheath tube not to extend beyond the proximal end of the protective tube.
  • the inner wall of the protection tube has a protrusion extending toward the inside of the protection tube, and the protrusion constitutes the anti-drop structure.
  • the proximal end of the protective tube is sleeved with an anti-dropping buckle, and the anti-dropping buckle has a limiting portion extending toward the inside of the protective tube, and the limiting portion constitutes the anti-falling structure .
  • the proximal end of the protective tube is a flared structure, and the inner diameter of the flared structure gradually increases from the distal end to the proximal direction of the protective tube.
  • a second connecting portion is provided on the protective tube, and the second connecting portion is used to connect with the protective sleeve to limit the distance of the protective tube toward the protective tube relative to the protective sleeve. The axial displacement of the end.
  • the second connecting portion has a first limiting surface, and the first limiting surface protrudes from the outer peripheral surface of the protective tube;
  • the protective sleeve has a second limiting surface, and the first limiting surface The limiting surface is used for abutting against the second limiting surface to limit the axial displacement of the protective tube relative to the protective sleeve toward the distal end of the protective tube.
  • the first connecting portion includes a plurality of engaging teeth, and the plurality of engaging teeth are arranged on the inner wall of the protective cover along the circumferential direction of the protective cover, and are used for connecting with the implant
  • the locking groove on the compression device matches.
  • the first connecting portion has an internal thread provided on the inner wall of the protective sleeve for matching with the external thread on the compression device of the implant.
  • a non-slip structure is provided on the outer wall of the protective cover.
  • the present invention also provides an implant compression device, which is used to cooperate with the above-mentioned implant loading tool, and the implant compression device includes:
  • the guide cover has a third connecting portion, and the third connecting portion is used for mating connection with the first connecting portion, so that the protection tube and the guide cover remain coaxial;
  • the guide seat is detachably connected with the guide cover to compress the implant.
  • the third connecting portion includes a plurality of engaging grooves, and the plurality of engaging grooves are provided on the outer wall of the guide cover along the circumferential direction of the guide cover, and are used to interact with the loading tool Match the engaging teeth on the
  • the third connecting portion has an external thread provided on the outer wall of the guide cover.
  • the guide cover has opposite first and second ends; the guide cover also has a first inner cavity through which the cross section of the first inner cavity extends from the first end to The second end gradually decreases; the guide seat has a third end and a fourth end opposite to each other; the guide seat is used to move from the third end to the fourth end along the direction from the third end to the fourth end. One end penetrates into the first inner cavity.
  • an implant loading system which includes:
  • a delivery device, the loading tool of the implant and the compression device of the implant are used to cooperate with the delivery device to load an implant in the delivery device; wherein, the protective tube
  • the proximal end of the guide cover is arranged face to face with the second end of the guide cover; the first connecting part of the protective sleeve is connected to the third connecting part of the guide cover, so that the protection tube and the guide cover Stay coaxial.
  • the implant is a valve stent; the delivery device includes a sheath, and the valve stent is used to be loaded into the sheath.
  • the implant loading tool is used to cooperate with an implant compression device to combine an implant Loaded into a delivery device
  • the loading tool of the implant includes a protective tube and a protective sleeve
  • the protective tube is used for the delivery device to pass through
  • the protective sleeve is connected to the compression device through the first connecting part
  • the detachable connection can keep the protection tube and the compression device coaxial.
  • FIG. 1 is a front view of a protective tube provided by Embodiment 1 of the present invention.
  • Figure 2 is an axial sectional view of the protective tube shown in Figure 1;
  • Figure 3 is a partial enlarged view of the protective tube shown in Figure 2;
  • FIG. 4 is a partial axial cross-sectional view of the protective tube provided by the second embodiment of the present invention.
  • Figure 5 is a front view of the protective cover provided by the first embodiment of the present invention.
  • Figure 6 is an axial sectional view of the protective sleeve shown in Figure 5;
  • FIG. 7 is a front view of a protective cover provided by Embodiment 2 of the present invention.
  • Figure 8 is an axial cross-sectional view of the protective sleeve shown in Figure 7;
  • Figure 9 is a front view of the guide cover provided in the first embodiment of the present invention.
  • Figure 10 is an axial sectional view of the guide cover shown in Figure 9;
  • Fig. 11 is a front view of a guide seat provided in the first embodiment of the present invention.
  • Figure 12 is an axial sectional view of the guide seat shown in Figure 11;
  • FIG. 13 is a schematic diagram of the guide cover and the guide base provided by the first embodiment of the present invention, wherein the fourth connecting portion of the guide cover is connected to the fifth connecting portion of the guide base;
  • Figure 14 is an axial sectional view of the guide cover and the guide seat shown in Figure 13;
  • FIG. 15 is a schematic diagram of a conveying device provided by Embodiment 1 of the present invention.
  • Figure 16 is a front view (partial cross-sectional view) of the loading system provided in the first embodiment of the present invention, in which the implant is about to be loaded into the sheath;
  • Figure 17 is an axial sectional view of the loading system shown in Figure 16;
  • Figure 18 is a partial enlarged view of the loading system shown in Figure 17;
  • 19 is an axial cross-sectional view of the loading system provided by the first embodiment of the present invention, in which the implant part has been loaded into the sheath;
  • Figure 20 is a partial enlarged view of the loading system shown in Figure 19;
  • 21 is an axial cross-sectional view of the loading system provided by the first embodiment of the present invention, in which the protective sleeve and the guide cover have moved to the distal end of the protective tube to expose the proximal end of the protective tube;
  • Fig. 22 is a schematic diagram of an implant provided in Embodiment 1 of the present invention.
  • 100-protection tube 101-proximal end; 102-distal; 110-anti-drop structure; 120-flaring structure; 130-first limit surface; 140-anti-drop buckle;
  • 300-guide cover 301-first end; 302-second end; 310-first inner cavity; 320-locking groove; 330-fourth connecting part; 331-tooth groove;
  • 400-guide seat 401-third end; 402-fourth end; 410-second inner cavity; 420-fixing groove; 430-fifth connecting part; 440-sixth connecting part;
  • 5-transport device 54-cone head; 55-fixed head; 56-sheath;
  • the invention provides a loading tool, a compression device and a loading system for an implant.
  • the loading tool of the implant is used to cooperate with a compression device of an implant to load an implant into a delivery device
  • the loading tool of the implant includes a protective tube and a protective sleeve; the protective tube is used for the delivery device to pass through, the protective tube has opposite proximal and distal ends, and the proximal end is used for For the implant to penetrate, the distal end is used for the delivery device to penetrate; the protective sleeve can be movably sleeved on the protective tube, and the protective sleeve is connected to the implant
  • the device remains coaxial. With such a configuration, no special person is required to fix the connecting part of the sheath and the implant, the loading tool
  • Figure 1 is a front view of the protective tube provided by Embodiment 1 of the present invention
  • Figure 2 is an axial sectional view of the protective tube shown in Figure 1
  • Figure 3 is the protective tube shown in Figure 2
  • Figure 4 is a partial axial cross-sectional view of the protective tube provided in the second embodiment of the present invention
  • Figure 5 is a front view of the protective sleeve provided in the first embodiment of the present invention
  • Figure 6 is the protective sleeve shown in Figure 5
  • Fig. 7 is a front view of the protective cover provided in the second embodiment of the present invention
  • Fig. 8 is an axial cross-sectional view of the protective cover shown in Fig. 7, and Fig.
  • FIG. 9 is the guide cover provided in the first embodiment of the present invention Front view
  • FIG. 10 is an axial cross-sectional view of the guide cover shown in FIG. 9
  • FIG. 11 is a front view of the guide seat provided by Embodiment 1 of the present invention
  • FIG. 12 is an axial cross-sectional view of the guide seat shown in FIG.
  • Figure 13 is a schematic diagram of the guide cover and the guide base provided by the first embodiment of the present invention, in which the fourth connecting portion of the guide cover is connected to the fifth connecting portion of the guide seat
  • Figure 14 is shown in Figure 13
  • Fig. 15 is a schematic diagram of the conveying device provided in the first embodiment of the present invention
  • Fig. 15 is a schematic diagram of the conveying device provided in the first embodiment of the present invention
  • FIG. 16 is a front view (partial cross-sectional view) of the loading system provided in the first embodiment of the present invention , Wherein the implant is about to be loaded into the sheath,
  • Figure 17 is an axial cross-sectional view of the loading system shown in Figure 16
  • Figure 18 is a partial enlarged view of the loading system shown in Figure 17
  • Figure 19 is the first embodiment of the present invention
  • FIG. 20 is a partial enlarged view of the loading system shown in FIG. 19, and FIG.
  • FIG 21 is an axial cross-sectional view of the loading system provided by Embodiment 1 of the present invention In the figure, the protective sleeve and the guide cover have moved to the distal end of the protective tube until the proximal end of the protective tube is exposed.
  • Figure 22 is a schematic diagram of the implant provided in the first embodiment of the present invention.
  • This embodiment provides an implant loading tool for cooperating with an implant compression device to load an implant into a delivery device
  • the loading tool for the implant includes a protective tube 100 and a protective sleeve 200.
  • the protective tube 100 has a proximal end 101 and a distal end 102 opposite to each other. The proximal end 101 and the distal end 102 are opposite to the protective tube 100.
  • the protective tube 100 is used for a delivery device to pass through (the delivery device preferably includes a sheath that passes through the protective tube 100), wherein the proximal end 101 is used for For an implant to penetrate, the distal end 102 is used for the delivery device to penetrate; the protective sleeve 200 is movably sleeved on the protective tube 100. And the protective cover 200 has a first connecting portion, the first connecting portion is used to detachably connect with the compression device of the implant, when the first connecting portion is connected with the compression device of the implant The protective sleeve 200 can be used to keep the protective tube 100 coaxial with respect to the compression device.
  • this embodiment provides an implant compression device, which is used to cooperate with a loading tool of the implant.
  • the compression device of the implant includes a guide cover 300 and a guide seat 400; the guide cover 300 has a third connecting portion, and the third connecting portion is used for mating connection with the first connecting portion, In order to keep the protective tube 100 and the guide cover 300 coaxial; the guide seat 400 and the guide cover 300 are detachably connected to compress the implant.
  • This embodiment also provides an implant loading system, which includes the above-mentioned implant loading tool and implant compression device, and also includes a delivery device 5, so
  • the delivery device 5 preferably includes a sheath 56.
  • the implant loading tool and the implant compression device are used to cooperate with the delivery device 5 to load the implant on the delivery device. 5 in the sheath 56; wherein, the proximal end 101 of the protective tube 100 and the second end 302 of the guide cover 300 are arranged face to face; the first connecting portion of the protective sleeve 200 and the guide cover 300
  • the third connecting part is connected to keep the protection tube 100 and the guide cover 300 coaxial.
  • a valve stent 9 is taken as an example of an implant to describe in detail the loading tool, compression device, and loading system of the implant provided in this embodiment.
  • the valve stent 9 includes an outflow channel 92, an inflow channel 93 and a hanging ear 91.
  • the valve stent 9 is compressed by the loading system provided in this embodiment with the assistance of the delivery device 5 and loaded into the sheath 56 .
  • the valve stent 9 is delivered to the target area by the delivery device 5 through the catheter by the delivery device 5 in the contracted state and released, and expanded to the state shown in FIG. 22.
  • the implant here refers to a compressible implant, such as a heart valve stent, but is not limited to the valve stent 9.
  • the present invention does not specifically limit the geometry and material of the implant, which can be Any existing implant in the art.
  • the protective tube 100 has a hollow inner cavity whose inner diameter matches the outer diameter of the sheath 56 (for example, the inner diameter of the protective tube 100 is slightly larger than that of the sheath 56 Outer diameter) for the sheath 56 to be movably inserted.
  • the protective sleeve 200 has a protective sleeve inner cavity 210, and the inner diameter of the protective sleeve inner cavity 210 matches the outer diameter of the protective tube 100 (for example, the inner diameter of the protective sleeve inner cavity 210 is slightly larger than the outer diameter of the protective tube 100).
  • the protective sleeve 200 can be movably sleeved on the protective tube 100.
  • the two can move relatively axially and remain coaxial.
  • the radial displacement of the protective sleeve 200 relative to the protective tube 100 can be limited to ensure that when the protective sleeve 200 is connected to the third connecting portion of the guide cover 300 through the first connecting portion, the protective tube 100 has no radial displacement relative to the guide cover 300 .
  • the first connecting portion of the protective cover 200 includes a plurality of engaging teeth 220, and the plurality of engaging teeth 220 are circumferentially arranged at The inner wall of the protective sleeve 200;
  • the third connecting portion of the guide cover 300 includes a plurality of engaging grooves 320 which are circumferentially arranged on the outer wall of the guide cover 300; engaging teeth 220 and the engaging groove 320 have the same number, the size and position are matched, and the two can be engaged with each other to limit the protective cover 200 without axial displacement and radial displacement relative to the guide cover 300, and the protective cover 200 can pass the protection
  • the sleeve cavity 210 defines at least no radial displacement of the protective tube 100 relative to the guide cover 300, and preferably also defines no axial displacement of the protective tube 100 relative to the guide cover 300. More preferably, when the engaging teeth 220 are engaged with the engaging groove 320, the protective tube 100, the protective sleeve 200 and the guide cover
  • the proximal end 101 of the protective tube 100 is provided with a flaring structure 120; the inner diameter of the flaring structure 120 gradually increases from the distal end 102 of the protective tube 100 to the proximal end 101.
  • the maximum inner diameter b of the flared structure 120 is close to the proximal end 101; the minimum inner diameter of the flared structure 120 is equal to the inner diameter c of the protective tube 100.
  • the valve stent 9 will be compressed from the expanded state and loaded into the sheath 56. The end (the head end) of the sheath 56 facing the valve stent 9 is received by the valve stent.
  • the head end With the effect of radial supporting force, the head end will undergo a slight morphological change (expansion). At this time, the presence of the flaring structure 120 provides support for the head end of the sheath 56. The mouth structure 120 fits together to prevent the head end of the sheath tube 56 from being over-expanded and damaged.
  • the flaring structure 120 can provide the valve stent 9 with compressive strain during the compression process of the valve stent 9 to reduce the Wear of the valve stent 9.
  • the bus bar of the flaring structure 120 is not limited to the straight line in FIG. 3, but may also be a curve, such as a convex curve facing the inside of the protective tube 100, or a combination of straight lines and curves, etc. The present invention does not limit this.
  • the length of the flaring structure 120 in the axial direction is 10%-30% of the sheath length.
  • the proximal end 101 of the protective tube 100 is provided with an anti-dropping structure 110, and the anti-dropping structure 110 is used to limit the sheath tube 56 not to exceed the protective tube 100 during the process of loading the valve stent 9 Near-end 101.
  • the inner wall of the protective tube 100 has a protrusion extending toward the inside of the protective tube 100, and the protrusion constitutes the anti-drop structure 110.
  • the protruding portion has a ring shape and is arranged on the proximal end 101 of the protective tube 100 or an inner wall close to the proximal end 101.
  • the inner diameter a of the protrusion is slightly smaller than the inner diameter c of the protective tube 100, is greater than or equal to the outer diameter x of the sheath tube 56 in the normal state, and less than or equal to the outer diameter x'of the end of the sheath tube 56 in the expanded state.
  • the inner diameter a is greater than or equal to the outer diameter x of the sheath tube 56 in the normal state, which can ensure that the sheath tube 56 can pass through the protective tube 100 when the valve stent 9 is not loaded, so that the tapered head (the maximum outer diameter of the tapered head)
  • the outer diameter of the sheath tube 56 is substantially the same) can pass through the protective tube 100.
  • the purpose of setting the inner diameter a to be less than or equal to the outer diameter x'of the end of the sheath tube 56 in the expanded state is: during the loading process, due to the radial support force of the valve stent 9, the head end of the sheath tube 56 A slight morphological change, that is, expansion.
  • the outer diameter x'of the end of the sheath 56 in the expanded state is greater than the outer diameter x of the sheath 56 in the normal state, and only the end with the inner diameter a less than or equal to the sheath 56 is set
  • the outer diameter x'of the portion in the expanded state can limit the sheath 56 to the distal side of the protrusion.
  • the purpose of the anti-fall structure 110 is to make the sheath 56 penetrate through the distal end 102 and be confined to the inside of the protective tube 100 and not exceed the proximal end 101 when the valve stent 9 is loaded, so as to prevent the sheath 56 from exceeding the protective tube 100
  • the proximal end 101 of the valve is damaged when the valve stent 9 is loaded. Specifically, during the loading process of the valve stent 9, the valve stent 9 and the sheath 56 move towards each other.
  • the sheath tube 56 When the valve stent 9 is loaded into the sheath 56 During the process, the sheath tube 56 will have a movement tendency opposite to the movement direction of the valve stent 9, and under the blocking of the anti-fall structure 110, it can be ensured that the sheath tube 56 is confined to the inside of the protective tube 100 in the axial direction.
  • the inner diameter a of the raised portion is smaller than the inner diameter c of the protective tube 100, which means that the inner diameter of the raised portion is smaller than the inner diameter of the protective tube 100 and the adjacent part of the raised portion, and an expansion is provided at the proximal end 101 of the protective tube 100
  • the inner diameter a of the protrusion is smaller than the inner diameter b of the flared structure 120 near the proximal end 101.
  • the flaring structure 120 ensures that the inner diameter of the protrusion is not less than the inner diameter of the protective tube 100, the sheath 56 can be closer to the protective tube 100, and the radial position of the sheath 56 in the protective tube 100 is fixed, which is beneficial to realize protection.
  • the tube 100, the protective sleeve 200 and the compression device are coaxial; preferably, the protrusion of the anti-dropping structure 110, the flaring structure 120 and the protective tube 100 are integrally formed, which has a relatively high structural strength.
  • the protrusion may not be a ring shape but a plurality of protruding teeth distributed around the axis of the protection tube 100, which can also achieve similar effects.
  • the protective tube 100 is provided with a second connecting portion, the second connecting portion is used to connect with the protective sleeve 200 to limit the protective tube 100 opposite In the axial displacement of the protective sleeve 200 toward the distal end 102; preferably, the second connecting portion has a first limiting surface 130, and the first limiting surface 130 protrudes from the protective tube 100
  • the outer peripheral surface of the protective sleeve 200 has a second limiting surface 230, and the first limiting surface 130 is used to abut against the second limiting surface 230.
  • the two opposing first limiting surface 130 and the second limiting surface 230 are abutted to limit the protective tube 100 to the distance relative to the protective sleeve 200.
  • Axial displacement of end 102 As shown in FIGS. 3, 6 and 16, the protective tube 100 relative to the protective sleeve 200 is limited by the axial displacement from the proximal end 101 to the distal end 102 of the protective tube.
  • the protective tube 100 is defined in an axial direction (toward the distal end 102) relative to the protective sleeve 200.
  • Direction and radial degrees of freedom.
  • the part of the first connecting part in the protective sleeve 200 has a groove cavity with a larger inner diameter than the inner diameter of the inner cavity 210 of the protective sleeve, and the groove cavity is used to accommodate the outer peripheral surface of the protective tube 100.
  • the axial cross-sectional shape of the cavity includes, but is not limited to, rectangular or trapezoidal. It should be understood that the second connecting portion is not limited to using the first limit surface 130 to connect with the protective sleeve 200, and the protective tube 100 and the protective sleeve 200 can also be connected by means such as interference fit, threaded fit, or snap fit.
  • the protective tube 100 has no axial (direction toward the distal end 102) and radial degrees of freedom relative to the protective sleeve 200.
  • the outside of the protective cover 200 may be stepped to facilitate the operator to grasp and apply force, but the outer shape of the protective cover 200 is not limited to a stepped shape, and may also be a cylindrical shape, a cone shape or even an irregular shape. Etc., the present invention does not limit this.
  • the guide cover 300 has a first end 301 and a second end 302 opposite to each other, the guide cover 300 also has a first inner cavity 310 that penetrates, and the guide seat 400 has a third end 401 opposite to each other. And the fourth end 402; the guide seat 400 is used to penetrate the first inner cavity 310 from the first end 301 along the direction from the third end 401 to the fourth end 402 to form An assembly for compressing the valve stent 9.
  • the cross section of the first inner cavity 310 gradually decreases from the first end 301 to the second end 302.
  • the cross section of the first inner cavity 310 gradually decreases from the first end 301 to the second end 302, which means that the cross section of the first inner cavity 310 is from the first end 301 to the second end 302. A decreasing trend, but does not limit any cross-section of the first inner cavity 310 to be larger than the cross-section on the side closer to the second end 302 of the cross-section.
  • the first cavity 310 of the guide cover 300 includes a first area and a second area connected in sequence from the first end 301 to the second end 302; the horizontal direction of the first area and the second area
  • the cross-sections are all circular, and the inner diameter of the first zone remains unchanged along the axial direction of the guide cover 300 (ie, the e-section to the right in FIG. 10).
  • the inner diameter of the second zone decreases from the side close to the first end 301 to the side close to the second end 302 (that is, the inner diameter of the e section in FIG. 10 is larger than the inner diameter of the d section).
  • the generatrix of the second area (in geometric terms, the shape of the curved surface can be regarded as the trajectory of a moving line, and the moving line forming the curved surface is called the generatrix) can be a straight line or a curve, such as a convex toward the inside of the guide cover 300
  • the curve or the concave curve may also be a combination of a straight line and a curve.
  • the bus bar in the first zone and the bus bar in the second zone transition smoothly.
  • the first area is used to contact, abut or connect with the guide base 400, and the second area is used to compress the valve stent 9.
  • the end of the first zone close to the first end 301 is provided with a plurality of tooth grooves 331 in the circumferential direction, and an inter-groove portion is formed between every two tooth grooves 331, so that the first zone can It is conveniently connected to the guide base 400 by expansion.
  • the guiding cover 300 has a fourth connecting portion 330; the guiding seat 400 has a fifth connecting portion 430 and a sixth connecting portion 440, and the fifth connecting portion 430 is opposite to the sixth connecting portion 440. It is closer to the fourth end 402; wherein, the fourth connecting portion 330 is used to detachably connect with the fifth connecting portion 430 and the sixth connecting portion 440 to define the guide cover 300 The radial displacement and axial displacement relative to the guide seat 400.
  • connection action of the fourth connection portion 330 and the fifth connection portion 430 precedes the connection of the fourth connection portion 330 and the sixth connection portion 440, and the fourth connection The portion 330 and the sixth connecting portion 440 are connected after the fourth connecting portion 330 and the fifth connecting portion 430 are separated.
  • the guide cover 300 and the guide seat 400 have no radial displacement, and the axial displacement is also limited and in a coaxial and stable state, which facilitates the tapering of the conveying device 5
  • the insertion of the head 54 facilitates the next compression of the valve stent 9 and also prevents the valve stent 9 from tilting or abrasion during the compression process.
  • the fourth connecting portion 330 is connected to the sixth connecting portion 440, that is, when the fourth connecting portion 330 is connected to the fifth connecting portion 430, the guiding seat 400 is deeper into the first inner cavity 310 of the guiding cover 300. The assembled body formed at this time completes the preliminary compression of the valve support 9.
  • the fourth connecting portion 330 includes a plurality of buckles arranged near the first end 301 in the inter-slot portion, and the fifth connecting portion 430 and the sixth connecting portion 440 are both connected to the buckles of the fourth connecting portion 330.
  • a matching buckle seat (such as a ring-shaped groove provided along the circumference of the guide seat 400).
  • the guide cover 300 and the guide seat 400 are connected by the way of matching and snapping of the buckle and the buckle seat, which is convenient for assembly and operation, and easy for disassembly, which improves the compression efficiency of the valve support 9. Because the first area of the guide cover 300 is divided into a plurality of sub-parts in the circumferential direction by a plurality of tooth grooves 331.
  • the multiple sub-parts are easy to be elastically deformed under the guidance of the guide seat 400 to guide the outside of the cover 300 in the radial direction. Expand until the buckle of the fourth connecting portion 330 matches with the buckle seat of the fifth connecting portion 430 or the sixth connecting portion 440, and the guide seat 400 is restricted to have no radial displacement relative to the guide cover 300. It can be understood that the number of the tooth grooves 331 can be selected according to needs, such as 2-12.
  • the tooth grooves 331 are preferably evenly distributed around the circumference of the guide cover 300, so that the plurality of grooves are symmetrically distributed in the circumference of the guide cover 300, such as axial symmetry, center symmetry, or rotational symmetry.
  • the buckle of the fourth connecting portion 330 can be provided on all the slots, preferably only on part of the slots, so as to ensure coaxial fixation and easy disassembly; more preferably Yes, the buckles are symmetrically distributed around the circumferential center of the guide cover 300 to ensure that the guide cover 300 and the guide seat 400 receive a uniform force when combined with the guide seat 400 without tilting.
  • the fourth connecting portion 330 and the fifth connecting portion 430 and the sixth connecting portion 440 may also be connected by friction fixing or interference fit, which is not limited in the present invention.
  • the guide seat 400 has a second inner cavity 410 penetrating in the axial direction, and the cross section of the second inner cavity 410 gradually decreases from the third end 401 to the fourth end 402 .
  • the cross-section of the second inner cavity 410 gradually decreases from the third end 401 to the fourth end 402, which also means that the changing trend is gradually reduced and not limited.
  • the second inner cavity 410 includes a third area and a fourth area connected from the third end 401 to the fourth end 402; the inner diameter of the third area near the third end 401 is larger than that of the third end 401.
  • the third area is close to the inner diameter of the fourth end 402; the inner diameter of the fourth area close to the third end 401 is equal to the inner diameter of the third area close to the fourth end 402, and is not less than the inner diameter of the fourth end 402.
  • the four regions are close to the inner diameter of the fourth end 402.
  • the third zone is used to compress the implant.
  • the cross-sections of the third zone and the fourth zone are both circular, and the bus bars of the third zone and the fourth zone are both straight lines, that is, the third zone has a larger bottom surface facing the third end 401 Round cone shape, the fourth area is cylindrical or round cone shape. More preferably, there is a smooth transition between the bus bars of the third zone and the fourth zone.
  • the second inner cavity 410 configured in this way is used to compress the valve stent 9 and can achieve better results.
  • busbars of the third zone and the fourth zone may not be smoothly transitioned, but a straight line is hardly connected to form a corner; or, one or two of the busbars of the third zone and the fourth zone are curved, which is actually used It can also achieve better results, and the present invention does not limit this.
  • the outer wall of the guide seat 400 is provided with a fixing groove 420 with an opening along the circumferential direction, and the opening of the fixing groove 420 faces the direction of the fourth end 402.
  • the fixing groove 420 is used for inserting and abutting the valve stent 9 (mainly the inflow channel 93 of the valve stent 9) to limit the axial displacement of the valve stent 9 toward the third end 401.
  • FIG. 15 is a delivery device 5, including a tapered head 54, a fixed head 55, a sheath 56, a catheter and a handle (not shown), the tapered head 54 is fixedly connected to the fixed head 55, and the fixed head 55
  • the sheath 56 is movably sleeved on the fixed head 55 under the control of the handle by connecting the connecting piece with the handle.
  • the fixing head 55 is used to connect with the hanging ear 91 of the valve support 9 as a force application end to apply force to the valve support 9.
  • the fixed head 55 is extended out of the sheath 56 through a handle operation.
  • the tapered head 54 is inserted into the second inner cavity 410 from the fourth end 402 of the guide seat 400 (at this time, the guide cover 300 and the guide seat 400 are in the first locked state, and the guide cover 300 and the guide seat 400 A valve holder 9) is installed between, and further, the hanging ear 91 is roughly aligned with the fixed head 55, and then the guide cover 300 is pushed in the direction of the guide seat 400, so that the fourth connecting part 330 and the sixth connecting part 440 is engaged to complete the further compression of the valve support 9.
  • part of the outflow channel 92 of the valve stent 9 and the hanging ears 91 are pushed out of the second end 302 of the guide cover 300 to form a fixed fit of the guide cover 300, the guide seat 400 and the valve stent 9 to facilitate Clip the hanging ear 91 in the groove of the fixed head 55.
  • the first connecting portion of the protective sleeve 200 and the third connecting portion of the guide cover 300 are connected to form a protective tube 100, a protective sleeve 200, and a guide
  • the cover 300 and the valve holder 9 are coaxial, which makes the hanging ear 91 and the groove of the fixed head 55 tightly combined, stable and reliable, and the operator can free his hands to operate the handle at the other end, realizing single operation.
  • the fixed head 55 drives the valve stent 9 toward the sheath 56
  • the internal movement of the valve stent 9 starts to be loaded into the sheath 56.
  • the valve stent 9 first touches the proximal end 101 of the protective tube 100, which prevents the valve stent 9 from directly squeezing and rubbing against the end of the sheath 56. Therefore, the protective tube 100 disperses the contact between the valve stent 9 and the sheath 56. The force exerted a protective effect on the sheath 56.
  • the tip end of the sheath tube 56 near the guide cap 300 (that is, the end where the valve stent 9 enters) will undergo a slight morphological change (expansion) due to the radial support force of the valve stent 9, and then fit the protective tube 100
  • the flaring structure 120 at the proximal end of the tube makes the protective tube 100 better protect the head end of the sheath tube 56.
  • the guide seat 400 and the guide cover 300 are separated, and the protective sleeve 200 and the guide cover 300 are both moved toward the distal end 102 of the protective tube 100 until the The proximal end 101 of the protective tube 100 (that is, the valve stent 9 is exposed) is used to load another part of the valve stent 9.
  • the protective cover 200 and the guide cover 300 can be separated from each other, or can be moved together as a whole.
  • the guiding base 400 is turned upside down (that is, the third end 401 And the direction of the fourth end 402), move the fourth end 402 to the third end 401 in the direction of the sheath 56 (left side in the figure), pass the third zone of the guide base 400, and move the valve stent
  • the inflow channel 93 of 9 is pushed into the fourth zone, so that the outer diameter of the inflow channel 93 is compressed to be close to the inner diameter of the sheath 56.
  • valve stent 9 is completely loaded into the sheath 56 and the entire valve stent 9 loading process is completed.
  • the first connecting portion of the protective sleeve 200 is connected with the third connecting portion of the guide cover 300 to make the protective tube 100 and the protective sleeve 200 ,
  • the guide cover 300 remains coaxial, which is beneficial to realize the fixing of the hanging ear 91 of the valve stent 9 to the fixed head 55, the loading tool and the compression device are fixed stably and firmly, and the operator can free his hands to operate the handle at the other end , A single person operation is realized.
  • the loading efficiency and the loading effect are further improved, and the valve stent 9 is prevented from tilting or breaking during the compression process.
  • the proximal end 101 of the protective tube 100 is provided with an anti-dropping buckle 140.
  • the material hardness of the anti-dropping buckle 140 is lower than that of the protective tube 100.
  • silica gel or rubber can be used.
  • the axial section of the anti-dropping buckle 140 is an L shape, one end is sleeved on the outer circumference of the proximal end 101 of the protection tube 100, and the other end of the L shape extends in the protection tube 100 along the radial direction of the protection tube 100 to form a limit position
  • the limiting portion forms the anti-dropping structure 110.
  • the limiting portion is preferably ring-shaped, and its inner diameter a is smaller than the inner diameter b of the proximal end 101 of the protective tube 100 adjacent to it.
  • the first connecting portion of the protective sleeve 200 has an internal thread 250 arranged on the inner wall of the protective sleeve 200, and to match it, in the compression device,
  • the third connecting portion has an external thread provided on the outer wall of the guide cover 300.
  • the protective sleeve 200 can be defined relative to the axis of the compression device. The radial displacement and the radial displacement can keep the protection tube 100 and the compression device fixed in the radial and axial directions.
  • a non-slip structure 240 is provided on the outer wall of the protective cover 200 to increase friction and facilitate the operator to grasp.
  • the anti-slip structure 240 can be, for example, an anti-slip groove or an anti-slip protruding tooth.
  • the present invention does not specifically limit the specific structure of the anti-slip structure 240, as long as it can facilitate grasping or increase the friction with the operator.

Landscapes

  • Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Transplantation (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Prostheses (AREA)
  • Media Introduction/Drainage Providing Device (AREA)

Abstract

L'invention concerne un instrument de chargement d'implant, un dispositif de compression et un système de chargement. L'instrument de chargement d'implant est conçu afin de coopérer avec le dispositif de compression d'implant afin de charger un implant dans un dispositif de pose (5). L'instrument de chargement d'implant comprend un tube de protection (100) et un manchon de protection (200). Le dispositif de pose (5) peut passer à travers le tube de protection (100), et le manchon de protection (200) est relié de façon détachable au dispositif de compression au moyen d'une première partie de liaison, de telle sorte que le tube de protection (100) et le dispositif de compression peuvent être maintenus coaxiaux. Une telle configuration rend plus stable la fixation de l'instrument de chargement au dispositif de compression et permet le maniement par une seule personne, de telle sorte que l'efficacité de chargement de l'implant est élevée, et le fonctionnement est relativement simple.
PCT/CN2020/072134 2019-01-24 2020-01-15 Instrument de chargement d'implant, dispositif de compression et système de chargement WO2020151538A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP20745653.4A EP3915520B1 (fr) 2019-01-24 2020-01-15 Instrument de chargement d'implant, dispositif de compression et système de chargement
KR1020217026401A KR102640498B1 (ko) 2019-01-24 2020-01-15 임플란트 로딩 도구, 압축 디바이스 및 로딩 시스템

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201910069078.1 2019-01-24
CN201910069078.1A CN111467080A (zh) 2019-01-24 2019-01-24 植入物的装载工具、压缩装置及装载系统

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WO2020151538A1 true WO2020151538A1 (fr) 2020-07-30

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EP (1) EP3915520B1 (fr)
KR (1) KR102640498B1 (fr)
CN (1) CN111467080A (fr)
WO (1) WO2020151538A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114760962A (zh) * 2020-10-29 2022-07-15 清流科技有限公司 用于将植入物转移到导管的连接器
EP4205704A4 (fr) * 2021-07-12 2024-04-17 Shanghai Trulive Medtech Co Ltd Système et procédé de chargement d'endoprothèse

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111467080A (zh) * 2019-01-24 2020-07-31 上海微创心通医疗科技有限公司 植入物的装载工具、压缩装置及装载系统
CN112618103B (zh) * 2020-12-07 2022-08-02 赛诺心畅医疗科技有限公司 一种可回收植入物的装载工具及装载方法
CN113648106A (zh) * 2021-06-28 2021-11-16 科凯(南通)生命科学有限公司 一种用于心脏瓣膜的装载工具
WO2024059254A1 (fr) * 2022-09-16 2024-03-21 Edwards Lifesciences Corporation Appareils d'aide au chargement de capsule et procédés associés

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101460115A (zh) * 2006-04-10 2009-06-17 可沃弗有限公司 用于将假体装载到最低程度侵入的输送系统的系统和方法
US20120330408A1 (en) * 2011-02-02 2012-12-27 St. Jude Medical, Inc. System for loading a collapsible heart valve
CN103517689A (zh) * 2011-05-05 2014-01-15 西美蒂斯股份公司 用于压缩/装载支架瓣膜的方法和设备
CN104586542A (zh) * 2013-10-31 2015-05-06 上海微创医疗器械（集团）有限公司 一种将植入体装载到输送系统中的装置和方法
CN204814285U (zh) * 2015-07-24 2015-12-02 上海微创医疗器械（集团）有限公司 植入体的装载装置
CN209827106U (zh) * 2019-01-24 2019-12-24 上海微创心通医疗科技有限公司 植入物的装载工具、压缩装置及装载系统

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4423730A (en) * 1982-03-01 1984-01-03 Shelhigh Inc. Atriotomy button and implantation device
EP2419050B2 (fr) * 2009-04-15 2023-10-18 Edwards Lifesciences CardiAQ LLC Implant vasculaire et système d'introduction
WO2012036742A2 (fr) 2010-09-17 2012-03-22 St. Jude Medical, Cardiology Division, Inc. Ensemble et procédé de chargement d'une valve cardiaque repliable auto-
CA3209217A1 (fr) * 2015-06-29 2017-01-05 Lyra Therapeutics, Inc. Systemes de chargement et de distribution de support
CN111467080A (zh) 2019-01-24 2020-07-31 上海微创心通医疗科技有限公司 植入物的装载工具、压缩装置及装载系统

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101460115A (zh) * 2006-04-10 2009-06-17 可沃弗有限公司 用于将假体装载到最低程度侵入的输送系统的系统和方法
US20120330408A1 (en) * 2011-02-02 2012-12-27 St. Jude Medical, Inc. System for loading a collapsible heart valve
CN103517689A (zh) * 2011-05-05 2014-01-15 西美蒂斯股份公司 用于压缩/装载支架瓣膜的方法和设备
CN104586542A (zh) * 2013-10-31 2015-05-06 上海微创医疗器械（集团）有限公司 一种将植入体装载到输送系统中的装置和方法
CN204814285U (zh) * 2015-07-24 2015-12-02 上海微创医疗器械（集团）有限公司 植入体的装载装置
CN209827106U (zh) * 2019-01-24 2019-12-24 上海微创心通医疗科技有限公司 植入物的装载工具、压缩装置及装载系统

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP3915520A4 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114760962A (zh) * 2020-10-29 2022-07-15 清流科技有限公司 用于将植入物转移到导管的连接器
CN114760962B (zh) * 2020-10-29 2023-06-06 清流科技有限公司 用于将植入物转移到导管的连接器
EP4205704A4 (fr) * 2021-07-12 2024-04-17 Shanghai Trulive Medtech Co Ltd Système et procédé de chargement d'endoprothèse

Also Published As

Publication number Publication date
EP3915520A4 (fr) 2022-03-16
EP3915520B1 (fr) 2024-04-10
CN111467080A (zh) 2020-07-31
KR20210118874A (ko) 2021-10-01
EP3915520C0 (fr) 2024-04-10
KR102640498B1 (ko) 2024-02-27
EP3915520A1 (fr) 2021-12-01

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